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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989171Generated: October 30, 2026

Water → 1-(3-Fluoro-5-iodophenylcarbamoyl)-5-methoxy-6-trifluoromethylindoline

https://huagongshe.com/reaction/989171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
Reactant3-Fluoro-5-iodoanilineHCID 2758986—
Reactant5-Methoxy-6-(trifluoromethyl)indolineHCID 11206713—
SolventDimethylformamideHCID 6228—
Product1-(3-Fluoro-5-iodophenylcarbamoyl)-5-methoxy-6-trifluoromethylindolineHCID 1800514340%

Reaction Steps

A mixture of 3-fluoro-5-iodoaniline (0.47 g, 1.98 mmol) and 1,1′-carbonyl imidazole (0.33 g, 2 mmol) in dichloromethane (40 ml) was stirred at room temperature for 1 h, then evaporated to dryness. To the residue was added dimethylformamide (DMF, 10 ml) and a solution of 5-methoxy-6-trifluoromethylindoline (D11, 0.44 g, 2 mmol) in DMF (5 ml). The mixture was heated at 80° C. overnight, then cooled and poured into water. The precipitate was filtered off, washed with water and dried. The crude product was chromatographed on silica gel and eluted with dichloromethane. Eluted product was recrystallised from dichloromethane to give the title compound (0.38 g, 40%), m.p. 221-4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638953B2
Source datasetuspto-grants-2003_10
ORD IDord-995d21a0a8da4ec2ad7b2d07f79c4377
Source noteuspto-grants-2003_10